Remote Job Hiring Document Review Specialist Medical Writing at Thermo Fisher. Apply for medical writing regulatory review pharma job opportunity today.
Company Overview
Thermo Fisher Scientific is a global leader in scientific research services, laboratory solutions, and clinical development. Through its PPD clinical research division, the company supports pharmaceutical and biotech organizations in accelerating drug development and improving patient outcomes worldwide. With clinical trials conducted across 100+ countries, Thermo Fisher continues to deliver cutting-edge solutions spanning laboratory, digital, and decentralized clinical research services.
The company is currently expanding its Medical Writing Functional Service Partnership (FSP) team and is hiring a Document Review Specialist II – Medical Writing for a fully remote role based in India. Remote Job Hiring Document Review Specialist Medical Writing at Thermo Fisher
Job Location & Employment Type
- Position: Document Review Specialist II – Medical Writing
- Company: Thermo Fisher Scientific (PPD Clinical Research)
- Location: Bangalore, India (Fully Remote)
- Employment Type: Full-Time
- Work Mode: Remote (Mon–Fri schedule)
- Job ID: R-01342111
This role is ideal for experienced medical writing or regulatory document professionals seeking flexible remote opportunities in global clinical research. Remote Job Hiring Document Review Specialist Medical Writing at Thermo Fisher
Department Details
- Division: PPD Clinical Research Services
- Function: Medical Writing / Regulatory Documentation Review
- Industry: CRO / Pharmaceutical Research
- Experience Level: Mid-Level (2+ years)
The selected candidate will review high-impact regulatory and clinical documents while collaborating with global clients.
Key Roles & Responsibilities
The Document Review Specialist will ensure scientific accuracy, clarity, and compliance of regulatory and clinical documents.
Core Responsibilities
- Review technical scientific documents to ensure quality and regulatory compliance.
- Evaluate clinical and regulatory submissions for consistency and accuracy.
- Verify data presented in tables, figures, and listings against source materials.
- Edit documents for grammar, clarity, and consistency.
- Ensure adherence to templates, style guides, and industry standards.
Medical Writing Support
- Review documents such as clinical study reports (CSR), protocols, amendments, investigator brochures (IB), and safety narratives.
- Improve scientific flow, readability, and audience appropriateness.
- Collaborate with authors and stakeholders to resolve content queries.
- Apply current regulatory guidelines and editorial standards.
- Manage priority reviews and dynamic timelines.
Quality & Compliance Responsibilities
- Maintain knowledge of global regulatory requirements and writing standards.
- Ensure alignment with ICH, GCP, and international regulatory frameworks.
- Follow structured review processes for consistency across deliverables.
- Support operational excellence through high-quality document reviews.
Remote Job Hiring Document Review Specialist Medical Writing at Thermo Fisher
Eligibility Criteria
Education
- Bachelor’s degree or equivalent qualification (mandatory)
- Degree in Life Sciences, Pharmacy, Biotechnology, or related fields preferred
Experience
- Minimum 2+ years of experience reviewing regulatory documents such as:
- Clinical Study Reports (CSR)
- Protocols and amendments
- Investigator Brochures (IB)
- Informed Consent Forms (ICF)
Experience in pharmaceutical or CRO environments is preferred. Remote Job Hiring Document Review Specialist Medical Writing at Thermo Fisher
Skills Required
- Strong understanding of medical writing and document review workflows
- Knowledge of GCP, ICH guidelines, and global regulatory requirements
- Familiarity with regulatory document structures
- Excellent English writing and editing skills
- Strong attention to detail and analytical thinking
- Good understanding of medical terminology and statistical concepts
- Proficiency in document formatting and Microsoft Word tools
- Experience with document management systems
Preferred Skills
- CRO client-dedicated project experience
- Experience working with multiple global stakeholders
- Advanced formatting and template compliance expertise
- Strong collaboration skills in virtual teams
- Ability to manage cross-cultural global projects
Remote Job Hiring Document Review Specialist Medical Writing at Thermo Fisher
Salary & Benefits
- Salary: As per company norms
- Benefits may include:
- Fully remote working model
- Competitive compensation and benefits package
- Global exposure in clinical research
- Learning and development programs
- Strong work-life balance culture
- Collaborative international work environment
Selection Process
The hiring process typically includes:
- Resume screening
- Technical interview (medical writing and review expertise)
- Client or stakeholder interaction
- Final selection and onboarding
Shortlisted candidates will be contacted by Thermo Fisher’s recruitment team. Remote Job Hiring Document Review Specialist Medical Writing at Thermo Fisher
How to Apply
- Application Mode: Online application via Thermo Fisher careers portal
- Candidates should apply with an updated resume highlighting regulatory writing and review experience.
Important Dates
- Application Deadline: Not specified
Early application is recommended due to high demand for remote medical writing roles. Remote Job Hiring Document Review Specialist Medical Writing at Thermo Fisher
Why Apply for This Pharma Job?
This remote Document Review Specialist role at Thermo Fisher offers an excellent opportunity for professionals seeking global exposure in medical writing while enjoying work-from-home flexibility.
Key Advantages
- Fully remote global CRO role
- Work with a leading clinical research organization
- Exposure to international regulatory documentation
- Strong career growth in medical writing and regulatory affairs
- Collaborative and flexible work culture
This role is ideal for professionals looking to advance their careers in regulatory writing without relocating. Remote Job Hiring Document Review Specialist Medical Writing at Thermo Fisher
Important Note / Disclaimer
IndiaPharmaJobs.in is an independent job information platform that shares verified pharmaceutical and clinical research job updates for informational purposes only. We are not affiliated with Thermo Fisher Scientific or its recruitment partners. Candidates should apply only through the official company website and should never pay any fees for job applications. Remote Job Hiring Document Review Specialist Medical Writing at Thermo Fisher
Final Words
If you have experience reviewing regulatory and clinical documents and are looking for a remote opportunity with a global CRO leader, this Document Review Specialist II role at Thermo Fisher is a strong career move. With international exposure, flexible work arrangements, and strong professional growth potential, the role provides an excellent platform for advancing your medical writing career. Interested candidates should apply online at the earliest to maximize their chances of selection. Remote Job Hiring Document Review Specialist Medical Writing at Thermo Fisher
